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A solution contains \(2.0 \times 10^{-4} \mathrm{MAg}^{+}\) and \(1.5 \times 10^{-3} \mathrm{M}\) \(\mathrm{Pb}^{2+}\). If NaI is added, will AgI \(\left(K_{s p}=8.3 \times 10^{-17}\right)\) or \(\mathrm{PbI}_{2}\) \(\left(K_{s p}=7.9 \times 10^{-9}\right)\) precipitate first? Specify the concentration of \(1^{-}\) needed to begin precipitation.

Short Answer

Expert verified
AgI will precipitate first when NaI is added to the solution. The concentration of I鈦 needed to begin precipitation is \(4.15 \times 10^{-13}\) M.

Step by step solution

01

Calculate the reaction quotient (Q) for each compound.

The reaction quotient, Q, can be calculated using the ion concentrations in solution. For each compound, Q is given by: AgI: \(Q_{1}= \mathrm{[Ag^{+}][I^{-}]} \) PbI鈧: \(Q_{2}=\mathrm{[Pb^{2+}][I^{-}]}^2 \) Initially, the I鈦 concentration is 0.
02

Compare the Q values to the Ksp values to determine which compound will precipitate first.

From the given information, we know: Ag鈦 concentration = \(2.0 \times 10^{-4}\) M Pb虏鈦 concentration: = \(1.5 脳 10^{-3}\) M We will compare the Ksp values for AgI and PbI鈧. The lower Ksp indicates the relative ease of precipitation. Ksp for AgI: \(8.3 \times 10^{-17}\) Ksp for PbI鈧: \(7.9 \times 10^{-9}\) Since Ksp(AgI) < Ksp(PbI鈧), AgI will precipitate first.
03

Calculate the concentration of I鈦 needed for the first compound to precipitate.

Now, we need to find the concentration of I鈦 needed for AgI to precipitate first. To do this, we set Q equal to the Ksp for AgI and solve for the I鈦 concentration: \[Q_{1} = K_{s p} (\mathrm{AgI})\] \[\mathrm{[Ag^{+}][I^{-}]}= 8.3 \times 10^{-17} \] \[\Rightarrow [I^{-}]=\frac{8.3 \times 10^{-17}}{\mathrm{[Ag^{ + }]}}\] \[ [I^{-}]=\frac{8.3 \times 10^{-17}}{2.0 \times 10^{-4}} \] Now, calculating the concentration of I鈦: \[ [I^{-}] = 4.15 \times 10^{-13} \mathrm{M} \] So, the concentration of I鈦 needed to begin precipitation is \(4.15 \times 10^{-13}\) M. AgI will precipitate first when NaI is added to the solution.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Solubility Product Constant (Ksp)
The solubility product constant, denoted as \( K_{sp} \), is a crucial concept in understanding solubility and precipitation reactions. It describes the equilibrium state between a solid and its ions in solution. Essentially, \( K_{sp} \) is a measure of how much of a compound can dissolve in water. For a generic salt \( AB \), which dissociates into \( A^+ \) and \( B^- \) ions, the \( K_{sp} \) expression is written as: \[ K_{sp} = [A^+][B^-] \] When a solution reaches the point where no more solute can dissolve, it鈥檚 at equilibrium, and the product of the ion concentrations equals \( K_{sp} \).
  • If the product of the ion concentrations in a solution exceeds \( K_{sp} \), the solution is supersaturated, and a precipitate will form.
  • If the ion product is less than \( K_{sp} \), the solution is unsaturated, and no precipitate will form.
In our example, the \( K_{sp} \) values for AgI and PbI鈧 suggest that AgI will precipitate first because its \( K_{sp} \) is much lower, indicating it's less soluble.
Precipitation Reactions
Precipitation reactions occur when dissolved ionic species in a solution combine to form an insoluble solid, or precipitate. Understanding when a precipitation reaction happens involves comparing the current state of the solution to the solubility product constant (\( K_{sp} \)). Here鈥檚 the basic process:
  • Initially, ions are freely moving in the solution. When the specific ion concentrations reach or exceed a certain level, they combine to form a solid.
  • For example, if iodine ions (\( I^- \)) are added to a solution containing silver ions (\( Ag^+ \)), they'll form AgI if the product \( [Ag^+][I^-] \) equals or surpasses the \( K_{sp} \).
In the case of AgI and PbI鈧, since AgI has a lower \( K_{sp} \), it means that less iodine is needed for it to start precipitating compared to PbI鈧. Thus, adding \( NaI \) to the solution will cause AgI to appear first as a solid.
Reaction Quotient (Q)
The reaction quotient \( Q \) is a valuable tool in predicting whether precipitation will occur in a solution. It helps to determine the current state of a reaction relative to its equilibrium by using the initial concentrations of the reacting species. The formula for \( Q \) mirrors the equilibrium expression, which, for AgI for example, would be: \[ Q = [Ag^+][I^-] \] By comparing \( Q \) to \( K_{sp} \), you can determine the tendency for a reaction to proceed.
  • If \( Q < K_{sp} \), the solution is below saturation, meaning no precipitate will form yet as the solution can still dissolve more ions.
  • If \( Q = K_{sp} \), the system is at equilibrium, and the solution is just saturated.
  • If \( Q > K_{sp} \), the solution is supersaturated, hence a precipitate will form.
In our exercise, we calculated \( Q \) for both AgI and PbI鈧 by setting it equal to the \( K_{sp} \) and solving for \( [I^-] \) to find the ion concentration needed to begin precipitation. This, in turn, allows us to predict which compound will precipitate from the solution first.

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Most popular questions from this chapter

A buffer is prepared by adding \(20.0 \mathrm{~g}\) of sodium acetate \(\left(\mathrm{CH}_{3} \mathrm{COONa}\right)\) to \(500 \mathrm{~mL}\) of a \(0.150 \mathrm{M}\) acetic acid \(\left(\mathrm{CH}_{3} \mathrm{COOH}\right)\) solution. (a) Determine the \(\mathrm{pH}\) of the buffer. (b) Write the complete ionic equation for the reaction that occurs when a few drops of hydrochloric acid are added to the buffer. (c) Write the complete ionic equation for the reaction that occurs when a few drops of sodium hydroxide solution are added to the buffer.

How many microliters of \(1.000 \mathrm{M} \mathrm{NaOH}\) solution must be added to \(25.00 \mathrm{~mL}\) of a \(0.1000 \mathrm{M}\) solution of lactic acid \(\left[\mathrm{CH}_{3} \mathrm{CH}(\mathrm{OH}) \mathrm{COOH}\right.\) or \(\left.\mathrm{HC}_{3} \mathrm{H}_{5} \mathrm{O}_{3}\right]\) to produce a buffer with \(\mathrm{pH}=3.75 ?\)

A solution of \(\mathrm{Na}_{2} \mathrm{SO}_{4}\) is added dropwise to a solution that is \(0.010 \mathrm{M}\) in \(\mathrm{Ba}^{2+}\) and \(0.010 \mathrm{M}\) in \(\mathrm{Sr}^{2+}\). (a) What con- centration of \(\mathrm{SO}_{4}^{2-}\) is necessary to begin precipitation? (Neglect volume changes. \(\mathrm{BaSO}_{4}: K_{s p}=1.1 \times 10^{-10} ; \mathrm{SrSO}_{4}:\) \(\left.K_{s p}=3.2 \times 10^{-7} .\right)\) (b) Which cation precipitates first? (c) What is the concentration of \(\mathrm{SO}_{4}^{2-}\) when the second cation begins to precipitate?

\(\begin{array}{llll}& \text { (a) If the molar solubility of } & \mathrm{CaF}_{2} & \text { at } & 35^{\circ} \mathrm{C} & \text { is }\end{array}\) \(1.24 \times 10^{-3} \mathrm{~mol} / \mathrm{L},\) what is \(K_{s p}\) at this temperature? (b) It is found that \(1.1 \times 10^{-2}\) of \(\mathrm{SrF}_{2}\) dissolves per \(100 \mathrm{~mL}\) of aqueous solution at \(25^{\circ} \mathrm{C} .\) Calculate the solubility product for \(\mathrm{SrF}_{2}\). (c) The \(K_{s p}\) of \(\mathrm{Ba}\left(\mathrm{IO}_{3}\right)_{2}\) at \(25^{\circ} \mathrm{C}\) is \(6.0 \times 10^{-10} .\) What is the molar solubility of \(\mathrm{Ba}\left(\mathrm{IO}_{3}\right)_{2}\) ?

How many milliliters of \(0.105 \mathrm{M} \mathrm{HCl}\) are needed to titrate each of the following solutions to the equivalence point: (a) \(45.0 \mathrm{~mL}\) of \(0.0950 \mathrm{M} \mathrm{NaOH},\) (b) \(22.5 \mathrm{~mL}\) of \(0.118 \mathrm{M} \mathrm{NH}_{3},(\mathrm{c})\) \(125.0 \mathrm{~mL}\) of a solution that contains \(1.35 \mathrm{~g}\) of \(\mathrm{NaOH}\) per liter?

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